Analysis of a pedigree of Peutz-Jeghers syndrome and RET proto-oncogene mutation: one case report and literature review

Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant inherited disorder characterised by gastrointestinal (GI) hamartomatous polyposis and mucocutaneous pigmentations. PJS is associated with an increased cancer risk, including GI and various extra-GI malignancies. In this study, we tracked this...

Descripción completa

Detalles Bibliográficos
Autores principales: Tian, Ling-Lin, Guo, Jun-Zhi, Yin, Yun-Qin, Dang, Xiao-Hong, Huo, Li-Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797457/
https://www.ncbi.nlm.nih.gov/pubmed/35117658
http://dx.doi.org/10.21037/tcr.2020.02.64

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797457/
https://www.ncbi.nlm.nih.gov/pubmed/35117658
http://dx.doi.org/10.21037/tcr.2020.02.64

Ejemplares similares